A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247083



Internal ID21309894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:34637053..34638890hg38UCSC Ensembl
Outerchr1:34626073..34648667hg38UCSC Ensembl
Innerchr1:35102654..35104491hg19UCSC Ensembl
Outerchr1:35091674..35114268hg19UCSC Ensembl
Innerchr1:34875241..34877078hg18UCSC Ensembl
Outerchr1:34864261..34886855hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3822595
hg1922595
hg1822595
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169465
Supporting Variants
SamplesNGO_53
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247083
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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